about
Dysbindin-1 is a synaptic and microtubular protein that binds brain snapinbeta-dystrobrevin, a member of the dystrophin-related protein familyDifferent dystrophin-like complexes are expressed in neurons and gliaAnimal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapyRole of mental retardation-associated dystrophin-gene product Dp71 in excitatory synapse organization, synaptic plasticity and behavioral functions.Loss of perivascular aquaporin 4 may underlie deficient water and K+ homeostasis in the human epileptogenic hippocampus.Components of the basal lamina and dystrophin-dystroglycan complex in the neurointermediate lobe of rat pituitary gland: different localizations of beta-dystroglycan, dystrobrevins, alpha1-syntrophin, and aquaporin-4.Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies.The DTNBP1 (dysbindin-1) gene variant rs2619522 is associated with variation of hippocampal and prefrontal grey matter volumes in humans.Three-dimensional regulation of radial glial functions by Lis1-Nde1 and dystrophin glycoprotein complexes.The sarcoglycan-sarcospan complex localization in mouse retina is independent from dystrophins.Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains.Dystrophin and utrophin isoforms are expressed in glia, but not neurons, of the avian parasympathetic ciliary ganglionThe roles of the dystrophin-associated glycoprotein complex at the synapseDysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophreniaMolecular and functional heterogeneity of GABAergic synapses.Cognitive dysfunction in Duchenne muscular dystrophy: a possible role for neuromodulatory immune molecules.Proton Magnetic Resonance Spectroscopy Indicates Preserved Cerebral Biochemical Composition in Duchenne Muscular Dystrophy Patients.A deficit of brain dystrophin impairs specific amygdala GABAergic transmission and enhances defensive behaviour in mice.The shortest isoform of dystrophin (Dp40) interacts with a group of presynaptic proteins to form a presumptive novel complex in the mouse brain.Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy.Dystrophin and beta-dystroglycan in photoreceptor terminals from normal and mdx3Cv mouse retinae.Facilitated NMDA receptor-mediated synaptic plasticity in the hippocampal CA1 area of dystrophin-deficient mice.Decrease in prosaposin in the Dystrophic mdx mouse brain.Increased vulnerability to kainate-induced seizures in utrophin-knockout mice.Dysregulation of Intracellular Ca2+ in Dystrophic Cortical and Hippocampal Neurons.Reorganization of inhibitory synapses and increased PSD length of perforated excitatory synapses in hippocampal area CA1 of dystrophin-deficient mdx mice.Development of a New Self-Reporting Instrument Measuring Benefits and Side Effects of Corticosteroids in Duchenne Muscular Dystrophy: Report from a Pilot Study.Sensorimotor control of breathing in the mdx mouse model of Duchenne muscular dystrophy.Cognitive flexibility deficits in a mouse model for the absence of full-length dystrophin.Amitriptyline is efficacious in ameliorating muscle inflammation and depressive symptoms in the mdx mouse model of Duchenne muscular dystrophy.Specific profiles of neurocognitive and reading functions in a sample of 42 Italian boys with Duchenne Muscular Dystrophy.Influence of full-length dystrophin on brain volumes in mouse models of Duchenne muscular dystrophy.
P2860
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P2860
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Dystrophin in the nervous system.
@en
type
label
Dystrophin in the nervous system.
@en
prefLabel
Dystrophin in the nervous system.
@en
P2860
P1433
P1476
Dystrophin in the nervous system.
@en
P2093
P2860
P356
10.1111/J.1750-3639.1996.TB00783.X
P577
1996-01-01T00:00:00Z